Canonical Allele Identifier: CA578624052
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1554444460
gnomAD v2: 7-141673463-AG-A
gnomAD v4: 7-141973663-AG-A
MyVariant Identifiers: chr7:g.141673464del (hg19) chr7:g.141973664del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973664del , CM000669.2:g.141973664del GRCh38
NC_000007.13:g.141673464del , CM000669.1:g.141673464del GRCh37
NC_000007.12:g.141319933del NCBI36
NG_016141.1:g.5110del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27667del (MGAM) ENSP00000419372.1:n.-3+27667del
ENST00000547270.1:c.26del (TAS2R38) MANE Select ENSP00000448219.1:p.Thr9MetfsTer23
NM_176817.4:c.26del (TAS2R38) NP_789787.4:p.Thr9MetfsTer23
XM_011515783.1:c.*25-12732del (OR9A4) XP_011514085.1:n.*25-12732del
NM_176817.5:c.26del (TAS2R38) MANE Select NP_789787.5:p.Thr9MetfsTer23
Search 100 bp 5'
Search 100 bp 3'